GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Sinorhizobium meliloti 1021

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; N-methyl-L-amino acid dehydrogenase; EC 1.5.1.21; EC 1.4.1.17 (characterized)
to candidate SMa0265 SMa0265 dehydrogenase

Query= SwissProt::Q4U331
         (343 letters)



>FitnessBrowser__Smeli:SMa0265
          Length = 334

 Score =  145 bits (366), Expect = 1e-39
 Identities = 111/322 (34%), Positives = 147/322 (45%), Gaps = 21/322 (6%)

Query: 30  GTSPEVADVLAENCASAQRDGSHSHGIFRIPGYLSSLASGWVDGKAVPVVEDVG----AA 85
           G   + A + A     A+  G  SHG+ R+P  LS L  G  +    P     G    A+
Sbjct: 20  GVPADSARLQANLLLEAELRGLPSHGLQRLPLLLSRLDKGLAN----PTTRGNGTWRRAS 75

Query: 86  FVRVDACNGFAQPALAAARSLLIDKARSAGVAILAIRGSHHFAALWPDVEPFAEQGLVAL 145
           F+ VD   G     +  A  +     +  G+AI AIR ++H   L    E  A  GL+ +
Sbjct: 76  FLSVDGERGLGPVVMMDAMRVTRRILKETGLAIAAIRNANHMGMLAYYAEAAARDGLIGI 135

Query: 146 SMVNSMTCVVPHGARQPLFGTNPIAFGAPRAGGEPIVFDLATSAIAHGDVQIAAREGRLL 205
            M  S   V P G  Q L GTNP+A G P A G P V DLATS ++ G +   A  G  +
Sbjct: 136 VMSTSEALVHPFGGTQALIGTNPVAIGIP-AAGHPFVLDLATSIVSMGKINNHAMRGLAI 194

Query: 206 PAGMGVDRDGLPTQEPRAILDGGALLPFGGHKGSALSMMVELLAAGLTGGNFSFEFDWSK 265
           P G  VDRDG  T +P A    GA+ PFG  KG  L + +ELL A L G N + + + + 
Sbjct: 195 PPGWAVDRDGRATTDPHA-AQAGAIAPFGDAKGYGLGLAIELLVAALAGSNLAPDVNGTL 253

Query: 266 ---HPGAQTPWTGQLLIVIDPDKGAGQHFAQRSE----ELVRQLHGVGQERLPGDRRYLE 318
              HP  +    G LLI+IDP  GAG   A  +      L R L       +PGD     
Sbjct: 254 DDIHPANK----GDLLILIDPSAGAGSIPALAAYLDRLRLSRPLDPTQPVAIPGDGARAR 309

Query: 319 RARSMAHGIVIAQADLERLQEL 340
           RA +   GI + Q   + L  L
Sbjct: 310 RAAAAKTGIELPQPLFDHLTAL 331


Lambda     K      H
   0.320    0.137    0.412 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 325
Number of extensions: 24
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 343
Length of database: 334
Length adjustment: 28
Effective length of query: 315
Effective length of database: 306
Effective search space:    96390
Effective search space used:    96390
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory